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Satoru Noguchi

Showing results (61-70 of 170) with videos related to

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Human Genome Variation|August 8, 2018
A novel <i>LMNA</i> mutation identified in a Japanese patient with LMNA-associated congenital muscular dystrophyAkihiko Ishiyama, Aritoshi Iida, Shinichiro Hayashi, et al.
Annals of Neurology|March 11, 2011
TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathyWen-Chen Liang, Hiroaki Mitsuhashi, Etsuko Keduka, et al.
The Journal of Biological Chemistry|November 14, 2020
Mutant BIN1-Dynamin 2 complexes dysregulate membrane remodeling in the pathogenesis of centronuclear myopathyKenshiro Fujise, Mariko Okubo, Tadashi Abe, et al.
Muscle & Nerve|November 14, 2006
Unfolded protein response and aggresome formation in hereditary reducing-body myopathyTeerin Liewluck, Yukiko K Hayashi, Maki Ohsawa, et al.
Neuroscience Research|January 30, 2007
Characterization of lobulated fibers in limb girdle muscular dystrophy type 2A by gene expression profilingYoko Keira, Satoru Noguchi, Rumi Kurokawa, et al.
Journal of Neuropathology and Experimental Neurology|May 22, 2009
Defective myotilin homodimerization caused by a novel mutation in MYOT exon 9 in the first Japanese limb girdle muscular dystrophy 1A patientSherine Shalaby, Hiroaki Mitsuhashi, Chie Matsuda, et al.
Neuromuscular Disorders : NMD|November 27, 2004
Two novel CAV3 gene mutations in Japanese familiesKazuma Sugie, Kumiko Murayama, Satoru Noguchi, et al.
The American Journal of Pathology|March 2, 2006
Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuolesRitsuko Ozawa, Yukiko K Hayashi, Megumu Ogawa, et al.
Inorganic Chemistry|March 24, 2007
Antiferromagnetic or canted antiferromagnetic orderings of Fe(III) d spins of FeX4- ions in BEDT-TTFVO(S).FeX4 (X = Cl, Br) [BEDT-TTFVO(S) = bis(ethylenedithio)tetrathiafulvalenoquinone(-thioquinone)-1,3-dithiolemethide]Mingxing Wang, Xunwen Xiao, Hideki Fujiwara, et al.
Acta Neuropathologica|February 25, 2010
Congenital myotonic dystrophy can show congenital fiber type disproportion pathologyKayo Tominaga, Yukiko K Hayashi, Kanako Goto, et al.
Pageof 17

Showing results (61-70 of 170) with videos related to

Sort By:
Pageof 17
Human Genome Variation|August 8, 2018
A novel <i>LMNA</i> mutation identified in a Japanese patient with LMNA-associated congenital muscular dystrophyAkihiko Ishiyama, Aritoshi Iida, Shinichiro Hayashi, et al.
Annals of Neurology|March 11, 2011
TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathyWen-Chen Liang, Hiroaki Mitsuhashi, Etsuko Keduka, et al.
The Journal of Biological Chemistry|November 14, 2020
Mutant BIN1-Dynamin 2 complexes dysregulate membrane remodeling in the pathogenesis of centronuclear myopathyKenshiro Fujise, Mariko Okubo, Tadashi Abe, et al.
Muscle & Nerve|November 14, 2006
Unfolded protein response and aggresome formation in hereditary reducing-body myopathyTeerin Liewluck, Yukiko K Hayashi, Maki Ohsawa, et al.
Neuroscience Research|January 30, 2007
Characterization of lobulated fibers in limb girdle muscular dystrophy type 2A by gene expression profilingYoko Keira, Satoru Noguchi, Rumi Kurokawa, et al.
Journal of Neuropathology and Experimental Neurology|May 22, 2009
Defective myotilin homodimerization caused by a novel mutation in MYOT exon 9 in the first Japanese limb girdle muscular dystrophy 1A patientSherine Shalaby, Hiroaki Mitsuhashi, Chie Matsuda, et al.
Neuromuscular Disorders : NMD|November 27, 2004
Two novel CAV3 gene mutations in Japanese familiesKazuma Sugie, Kumiko Murayama, Satoru Noguchi, et al.
The American Journal of Pathology|March 2, 2006
Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuolesRitsuko Ozawa, Yukiko K Hayashi, Megumu Ogawa, et al.
Inorganic Chemistry|March 24, 2007
Antiferromagnetic or canted antiferromagnetic orderings of Fe(III) d spins of FeX4- ions in BEDT-TTFVO(S).FeX4 (X = Cl, Br) [BEDT-TTFVO(S) = bis(ethylenedithio)tetrathiafulvalenoquinone(-thioquinone)-1,3-dithiolemethide]Mingxing Wang, Xunwen Xiao, Hideki Fujiwara, et al.
Acta Neuropathologica|February 25, 2010
Congenital myotonic dystrophy can show congenital fiber type disproportion pathologyKayo Tominaga, Yukiko K Hayashi, Kanako Goto, et al.
Pageof 17